首页> 美国卫生研究院文献>Journal of Clinical Laboratory Analysis >Conversion of cardiac and liver transplant recipients from HPLC and FPIA (polyclonal) to an FPIA (monoclonal) technique for measurement of blood cyclosporin A
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Conversion of cardiac and liver transplant recipients from HPLC and FPIA (polyclonal) to an FPIA (monoclonal) technique for measurement of blood cyclosporin A

机译:将心脏和肝脏移植受者从HPLC和FPIA(多克隆)转换为FPIA(单克隆)技术以测量血液中的环孢菌素A

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摘要

In an effort to replace HPLC and FPIA (polyclonal) for whole blood determination of Cyclosporin A (CsA), this study examined the application of FPIA (monoclonal) in patients post cardiac and liver transplantation. The assay had a minimum detectable dose of 15μg/ L, an overall recovery of 97% and was linear to 1200μg/ L, and gave inter‐assay precision values of < 5% (CV). On comparing FPIA (monoclonal) and HPLC for 59 cardiac transplant recipient blood samples, a correlation of FPIA (monoclonal) = 1.30 (HPLC) + 36.34, r = 0.96 was obtained. With liver transplant samples (n = 348), the correlation was FPIA (monoclonal) = 1.21 (HPLC) + 42.15, r = 0.98. Correlation on 131 cardiac transplant recipients gave FPIA (monoclonal) = 0.31 FPIA (polyclonal) + 43.97, r = 0.68. It is concluded that when converting from HPLC to FPIA (monoclonal) a positive bias of 21%–30% is observed, and in replacing FPIA (polyclonal) with FPIA (monoclonal), a negative bias of 50%–69% is seen with liver and cardiac patients respectively. These data indicate that therapeutic ranges should be reestablished or adjustments in CsA dosing would be necessary. J. Clin. Lab. Anal. 12:337–342, 1998. © 1998 Wiley‐Liss, Inc.
机译:为了代替HPLC和FPIA(多克隆)来测定环孢菌素A(CsA)的全血,本研究研究了FPIA(单克隆)在心脏和肝脏移植术后患者中的应用。该测定法的最低可检测剂量为15μg/ L,总回收率为97%,与1200μg/ L呈线性关系,测定间精密度值<5%(CV)。比较59个心脏移植受者血液样本的FPIA(单克隆)和HPLC时,FPIA(单克隆)= 1.30(HPLC)+ 36.34,r = 0.96的相关性。对于肝移植样品(n = 348),相关性为FPIA(单克隆)= 1.21(HPLC)+ 42.15,r = 0.98。 131个心脏移植受者的相关性得出FPIA(单克隆)= 0.31 FPIA(多克隆)+ 43.97,r = 0.68。结论是,从HPLC转换为FPIA(单克隆)时,可观察到21%–30%的正偏差,而用FPIA(单克隆)替代FPIA(多克隆)时,则可观察到50%–69%的负偏差。肝脏和心脏病患者。这些数据表明应重新建立治疗范围,否则必须调整CsA剂量。 J.临床实验室肛门12:337–342,1998.©1998 Wiley-Liss,Inc.

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